SME - PHARMA Safety/ Pharmacovigilance - Onsite - Raritan, United States - The Dignify Solutions LLC

SME - PHARMA Safety/ Pharmacovigilance

3 weeks ago

POSITION: SME - PHARMA Safety/ Pharmacovigilance · LOCATION: Raritan, NJ (Day one onsite) · Job Description: · In this role consultant will be working as a SME on Safety/ Pharmacovigilance industry transformation group for pharma R&D value chain. · Will be mainly responsible t ...

Compliance Analyst

2 weeks ago

Source One is a consulting services company and we're currently looking for the following individual to work as a consultant with our direct client, a global Pharmaceutical Manufacturing Company. This is fully Remote position, however you may travel for a possible mandatory meeti ...

Compliance Analyst

1 week ago

Source One is a consulting services company and were currently looking for the following individual to work as a consultant with our direct client, a global Pharmaceutical Manufacturing Company. This is fully Remote position, however you may travel for a possible mandatory meetin ...

Supervisor, Patient Support

2 weeks ago

Overview: · **Program : Affordability / Fixer Program** · Under the direction of the department leader, the Supervisor, Patient Support is responsible for ensuring that their team provides extraordinary patient concierge health care services enabling access to care for prescripti ...

Analyst 2

1 week ago

Sr. Associate, Aggregate Report Compliance · Role can be 100% REMOTE · - May travel for a possible mandatory meeting onsite for 1-2 days, not very often at all · - Bachelors Degree required · - Pharmacovigilance experience needed · - Must be flexible / adaptive · - Must be able t ...

Analyst 2

2 weeks ago

Sr. Associate, Aggregate Report Compliance · Role can be 100% REMOTE · - May travel for a possible mandatory meeting onsite for 1-2 days, not very often at all · - Bachelors Degree required · - Pharmacovigilance experience needed · - Must be flexible / adaptive · - Must be ...

Analyst 2

1 week ago

Position Details: · Our client, a world-leading Pharmaceutical Company in Raritan, NJ is currently looking for a Drug Safety Associate (Aggregate Reports) to join their expanding team. · Job Title: Drug Safety Associate (Aggregate Reports) / Pharma Industry / REMOTE WORK · Durat ...

Associate Clinical Research Associate

2 weeks ago

**Position Description**: · With support of Sr CRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. · - Develops strong site relationships and ensures continuity of ...

Associate Clinical Research Associate

2 weeks ago

With support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. · - Develops strong site relationships and ensures continuity of site relationships through al ...

Data Architect with GCP AND LSS(Life Sciences Services) at Raritan, New Jersey

2 days ago

Job Description · Job DescriptionTitle: Data Architect with GCP and LSS(Life Sciences Services) · Type: Fulltime · Location: Raritan, New Jersey (Onsite) · Job Title: Data Architect for LSS · Own the end-to-end architecture of the modern Safety/Pharmacovigilance Data Platforms ...

Data Architect

12 hours ago

The Possibilities are Endless When You ChallengeTheNorm · Birlasoft combines the power of domain, enterprise, and digital technologies to reimagine business processes for customers and their ecosystem. Its consultative and design thinking approach makes societies more productive ...

GPV Case Management Product Specialist

2 weeks ago

Summary · Our growing, mid-sized pharmaceutical client has engaged GForce Life Sciences to provide a GPV Submission Specialist responsible for managing daily operational activities of the Global Submissions Team within Case processing. · Description · Monitor and manage the ICSR ...

Drug Safety Physician

3 weeks ago

The Project Physician tasks may include: · Contribute to writing and reviewing of study related documents such as: protocols, protocol amendments, informed consent forms, statistical analysis plans, clinical study reports, and other similar documents · Contribute to writing and r ...

Director, Epidemiology

3 weeks ago

Job Description · At Genmab, we're committed to building extra[not]ordinary futures together, by developing antibody products and pioneering, knock-your-socks-off therapies that change the lives of patients and the future of cancer treatment and serious diseases. From our people ...

GVP Auditor

3 weeks ago

The GPV Auditor will lead and perform audits with a focus on Pharmacovigilance activities. Additional tasks are required to support the continuous improvement of the Otsuka Quality System, inspection management, regulatory intelligence activities, SOP and WP management, validatio ...

GPV Specialist

2 weeks ago

Summary · Our growing, mid-sized pharmaceutical client has engaged GForce Life Sciences to provide a GPV Submission Specialist responsible for managing daily operational activities of the Global Submissions Team within Case processing. · Description · Monitor and manage the IC ...

IT Quality Compliance Specialist/Analyst

1 week ago

Innova Solutions is immediately hiring for an IT Quality Compliance Specialist/Analyst · Tittle- IT Quality Compliance Specialist/Analyst · Duration -6 months · Location-New Brunswick ,NJ (onsite) · Pay Range*: $ $79.71 per hour. · As a(n)IT Quality Compliance Specialist/Analy ...

PM/BA Global Pharmacovigilance

2 weeks ago

PM/BA Global Pharmacovigilance (GPV) · Location: Princeton, NJ · Day 1 Onsite. · We are looking for PM/BA resources with Global Pharmacovigilance (GPV) knowledge. · The efforts will require a team who is familiar with GPV space and is able to work closely with GPV and IT to f ...

GPV Specialist

1 week ago

Summary · Our growing, mid-sized pharmaceutical client has engaged GForce Life Sciences to provide a GPV Submission Specialist responsible for managing daily operational activities of the Global Submissions Team within Case processing. · Description · Monitor and manage the ICSR ...

GPV Submission Specialist

2 weeks ago

Consultant, GPV Case Management Product Specialist, Pharmaceuticals · Summary · Our growing, mid-sized pharmaceutical client has engaged GForce Life Sciences to provide a GPV Submission Specialist responsible for managing daily operational activities of the Global Submissions Te ...